HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413744Generated: October 31, 2026
Ethanol → Ethyl 2-isopropyl-5-oxo-1-imidazolidineacetate
https://huagongshe.com/reaction/2413744
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium 2-(1-methylethyl)-5-oxo-1-imidazolidineacetate | HCID 23672396 | — |
| Product | Ethyl 2-isopropyl-5-oxo-1-imidazolidineacetate | HCID 14618022 | 42% |
Reaction Steps
To 50 ml of anhydrous ethanol stirred at 0°-5° C., 2 ml thionyl chloride were added. At the same temperature 2.1 g (0.01 mol) of sodium 2-(1-methylethyl)-5-oxo-1imidazolidineacetate were added. The suspension obtained was stirred at 0° C. for 1 hour and at room temperature for 2 hours. The solvent was evaporated under reduced pressure and the residue taken up with ethyl acetate. The solid residue was filtered off and the solvent evaporated. The residue was dissolved in a saturated solution of sodium hydrogen carbonate and extracted with 3×50 ml of dichloromethane. The organic layers were dried and evaporated to give ethyl 2-(1-methylethyl)-5-oxo-1imidazolidineacetate (0.9 g) as a pale-yellow oil (42%) (Rf 0.6, ethyl acetate/dichloromethane 6:4; silica gel plates). Hydrochloride salt, m.p. 148°-149° C. (methanol/ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04719222 |
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| Source dataset | uspto-grants-1988_01 |
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| ORD ID | ord-29b8de90a7d2415094dad4ed0aabd579 |
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| Source note | uspto-grants-1988_01 |
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